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1.
Neuroimage ; 49(2): 1622-31, 2010 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-19837175

RESUMO

How little neurotransmission in the visual system is sufficient to promote decent visual capabilities? This question is of key importance for therapeutic approaches to restore vision in patients who suffer from degenerative retinal diseases. In the retinae of mice, mutant for the presynaptic scaffolding protein Bassoon (Bsn), signal transfer at photoreceptor ribbon synapses is severely disturbed due to impaired ribbon attachment to the active zone. We have used two different behavioural tasks and optical imaging of intrinsic signals to probe vision in young and adult Bsn-/- mice and their wild-type littermates. Here we show that while visual acuity was significantly reduced in mutants compared to controls, vision guided behavioural decisions and optical imaging revealed essentially unperturbed cortical signals and retinotopy in spite of the photoreceptor synaptopathy. In addition, both vision and visual cortical maps were adult-like at 4 weeks of age. These results show that (i) while Bassoon-dependent fast exocytosis is essential for normal vision surprisingly good visual performance can be achieved in the absence of synaptic ribbons, (ii) both the development and maintenance of visual cortical maps is independent of synaptic ribbons and (iii) visual development in the mutants is completed at 4 weeks of age indicating that later developing ectopic synapses do not affect vision. Thus, the central visual system can make use of slow and weak retinal signals to subserve surprisingly robust vision.


Assuntos
Células Fotorreceptoras de Vertebrados/fisiologia , Sinapses/fisiologia , Transtornos da Visão/fisiopatologia , Córtex Visual/fisiopatologia , Percepção Visual/fisiologia , Envelhecimento/fisiologia , Animais , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout , Proteínas do Tecido Nervoso/genética , Óptica e Fotônica/métodos , Retina/crescimento & desenvolvimento , Retina/fisiopatologia , Testes Visuais , Córtex Visual/irrigação sanguínea , Córtex Visual/crescimento & desenvolvimento , Vias Visuais/irrigação sanguínea , Vias Visuais/crescimento & desenvolvimento , Vias Visuais/fisiopatologia
2.
Eur J Neurosci ; 26(9): 2506-15, 2007 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-17970721

RESUMO

Knowledge about the plastic and regenerative capacity of the retina is of key importance for therapeutic approaches to restore vision in patients who suffer from degenerative retinal diseases. In the retinae of mice, mutant for the presynaptic scaffolding protein Bassoon, signal transfer at photoreceptor ribbon synapses is disturbed due to impaired ribbon attachment to the active zone. In a long-term study we observed, with light and electron microscopic immunocytochemistry and electroretinographic recordings, two overlapping events in the Bassoon mutant retina, i.e. loss of photoreceptor synapses in the outer plexiform layer, and structural remodeling and formation of ectopic photoreceptor synapses in the outer nuclear layer, a region usually devoid of synapses. Formation of ectopic synaptic sites starts around the time when photoreceptor synaptogenesis is completed in wild-type mice and progresses throughout life. The result is a dense plexus of ectopic photoreceptor synapses with significantly altered but considerable synaptic transmission. Ectopic synapse formation is led by the sprouting of horizontal cells followed by the extension of rod bipolar cell neurites that fasciculate with and grow along the horizontal cell processes. Although only the rod photoreceptors and their postsynaptic partners show structural and functional remodeling, our study demonstrates the potential of the retina for long-lasting plastic changes.


Assuntos
Regeneração Nervosa/genética , Plasticidade Neuronal/genética , Células Fotorreceptoras Retinianas Cones/fisiopatologia , Degeneração Retiniana/fisiopatologia , Células Fotorreceptoras Retinianas Bastonetes/fisiopatologia , Sinapses/genética , Animais , Diferenciação Celular/genética , Modelos Animais de Doenças , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Mutantes , Microscopia Imunoeletrônica , Proteínas do Tecido Nervoso/genética , Vias Neurais/patologia , Vias Neurais/fisiopatologia , Recuperação de Função Fisiológica/genética , Células Bipolares da Retina/patologia , Células Bipolares da Retina/fisiologia , Células Fotorreceptoras Retinianas Cones/patologia , Degeneração Retiniana/genética , Degeneração Retiniana/patologia , Células Horizontais da Retina/patologia , Células Horizontais da Retina/fisiopatologia , Células Fotorreceptoras Retinianas Bastonetes/patologia , Sinapses/ultraestrutura , Transmissão Sináptica/genética , Visão Ocular/genética
3.
Neuron ; 37(5): 775-86, 2003 Mar 06.
Artigo em Inglês | MEDLINE | ID: mdl-12628168

RESUMO

The photoreceptor ribbon synapse is a highly specialized glutamatergic synapse designed for the continuous flow of synaptic vesicles to the neurotransmitter release site. The molecular mechanisms underlying ribbon synapse formation are poorly understood. We have investigated the role of the presynaptic cytomatrix protein Bassoon, a major component of the photoreceptor ribbon, in a mouse retina deficient of functional Bassoon protein. Photoreceptor ribbons lacking Bassoon are not anchored to the presynaptic active zones. This results in an impaired photoreceptor synaptic transmission, an abnormal dendritic branching of neurons postsynaptic to photoreceptors, and the formation of ectopic synapses. These findings suggest a critical role of Bassoon in the formation and the function of photoreceptor ribbon synapses of the mammalian retina.


Assuntos
Proteínas do Tecido Nervoso/deficiência , Proteínas do Tecido Nervoso/fisiologia , Células Fotorreceptoras de Vertebrados/metabolismo , Terminações Pré-Sinápticas/metabolismo , Animais , Camundongos , Camundongos Mutantes , Proteínas do Tecido Nervoso/biossíntese , Proteínas do Tecido Nervoso/genética , Estimulação Luminosa/métodos , Células Fotorreceptoras de Vertebrados/ultraestrutura , Terminações Pré-Sinápticas/ultraestrutura , Retina/metabolismo , Retina/ultraestrutura , Sinapses/metabolismo , Sinapses/ultraestrutura
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